Canonical Allele Identifier: CA1577046901

Gene: HSD17B4

Linked Data

• dbSNP Id: rs1754067408

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119531227T>C , CM000667.2:g.119531227T>C	GRCh38
NC_000005.9:g.118866922T>C , CM000667.1:g.118866922T>C	GRCh37
NC_000005.8:g.118894821T>C	NCBI36
NG_008182.1:g.83775T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000509514.6:c.1786-39T>C	ENSP00000426272.2:n.1786-39T>C
ENST00000518349.6:c.1099-39T>C	ENSP00000507185.1:n.1099-39T>C
ENST00000682445.1:c.*1736-39T>C	ENSP00000508061.1:n.*1736-39T>C
ENST00000682531.1:n.3747-39T>C
ENST00000682626.1:c.*1361-39T>C	ENSP00000507857.1:n.*1361-39T>C
ENST00000682996.1:c.1783-39T>C	ENSP00000507792.1:n.1783-39T>C
ENST00000683265.1:n.3641-39T>C
ENST00000683335.1:n.3257-39T>C
ENST00000683371.1:c.*1985-39T>C	ENSP00000508376.1:n.*1985-39T>C
ENST00000683372.1:n.3865-39T>C
ENST00000683390.1:n.3545-39T>C
ENST00000683476.1:n.697-39T>C
ENST00000683549.1:n.3469-39T>C
ENST00000683936.1:c.*3433-39T>C	ENSP00000507721.1:n.*3433-39T>C
ENST00000683974.1:n.3584-39T>C
ENST00000683996.1:c.*1065-39T>C	ENSP00000507060.1:n.*1065-39T>C
ENST00000684131.1:n.3387-39T>C
ENST00000684160.1:c.*1545-39T>C	ENSP00000507821.1:n.*1545-39T>C
ENST00000684214.1:c.1854+1247T>C	ENSP00000508071.1:n.1854+1247T>C
ENST00000414835.7:c.1930-39T>C	ENSP00000411960.3:n.1930-39T>C
ENST00000510025.7:c.1855-39T>C MANE Select	ENSP00000424940.3:n.1855-39T>C
ENST00000643250.1:c.*1727-39T>C	ENSP00000494737.1:n.*1727-39T>C
ENST00000644146.1:c.*3126-39T>C	ENSP00000494808.1:n.*3126-39T>C
ENST00000645099.1:c.1414-39T>C	ENSP00000496091.1:n.1414-39T>C
ENST00000645702.1:c.*1258-39T>C	ENSP00000496432.1:n.*1258-39T>C
ENST00000645832.1:c.*1740-39T>C	ENSP00000494316.1:n.*1740-39T>C
ENST00000646058.1:c.1855-39T>C	ENSP00000493579.1:n.1855-39T>C
ENST00000646355.1:c.*1861-39T>C	ENSP00000493801.1:n.*1861-39T>C
ENST00000646554.1:c.*1833-39T>C	ENSP00000494542.1:n.*1833-39T>C
ENST00000647335.1:c.*1822-39T>C	ENSP00000495180.1:n.*1822-39T>C
ENST00000647342.1:c.*1786-39T>C	ENSP00000494992.1:n.*1786-39T>C
ENST00000256216.10:c.1855-39T>C	ENSP00000256216.6:n.1855-39T>C
ENST00000414835.6:c.1435-39T>C	ENSP00000411960.2:n.1435-39T>C
ENST00000442060.7:c.*410-39T>C	ENSP00000390208.3:n.*410-39T>C
ENST00000504811.5:c.1930-39T>C	ENSP00000420914.1:n.1930-39T>C
ENST00000509514.5:c.1069-39T>C	ENSP00000426272.1:n.1069-39T>C
ENST00000509606.1:n.150-39T>C
ENST00000509951.5:n.309+1247T>C
ENST00000510025.5:c.1783-39T>C	ENSP00000424940.1:n.1783-39T>C
ENST00000513628.5:c.1444-39T>C	ENSP00000425993.1:n.1444-39T>C
ENST00000515235.6:n.3608-39T>C
ENST00000515320.5:c.1801-39T>C	ENSP00000424613.1:n.1801-39T>C
ENST00000522415.5:n.522-39T>C
NM_000414.3:c.1855-39T>C	NP_000405.1:n.1855-39T>C
NM_001199291.2:c.1930-39T>C	NP_001186220.1:n.1930-39T>C
NM_001199292.1:c.1801-39T>C	NP_001186221.1:n.1801-39T>C
NM_001292027.1:c.1783-39T>C	NP_001278956.1:n.1783-39T>C
NM_001292028.1:c.1435-39T>C	NP_001278957.1:n.1435-39T>C
NM_000414.4:c.1855-39T>C MANE Select	NP_000405.1:n.1855-39T>C
NM_001199291.3:c.1930-39T>C	NP_001186220.1:n.1930-39T>C
NM_001199292.2:c.1801-39T>C	NP_001186221.1:n.1801-39T>C
NM_001292027.2:c.1783-39T>C	NP_001278956.1:n.1783-39T>C
NM_001292028.2:c.1435-39T>C	NP_001278957.1:n.1435-39T>C
NM_001374497.1:c.1846-39T>C	NP_001361426.1:n.1846-39T>C
NM_001374498.1:c.1783-39T>C	NP_001361427.1:n.1783-39T>C
NM_001374499.1:c.1528-39T>C	NP_001361428.1:n.1528-39T>C
NM_001374500.1:c.1414-39T>C	NP_001361429.1:n.1414-39T>C
NM_001374501.1:c.1444-39T>C	NP_001361430.1:n.1444-39T>C
NM_001374502.1:c.1444-39T>C	NP_001361431.1:n.1444-39T>C
NM_001374503.1:c.1444-39T>C	NP_001361432.1:n.1444-39T>C
NR_164653.1:n.1952-39T>C
NR_164654.1:n.2220-39T>C